About: chromosome 19q13.11 deletion syndrome

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease chromosomal deletion syndrome nodeID://b50938792
label	chromosome 19q13.11 deletion syndrome
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060408
created_by	elvira
creation_date	2015-09-28T17:09:44Z
database_cross_reference	GARD:10592 MESH:C567810 OMIM:613026 ORDO:217346 UMLS_CUI:C2751651
has_exact_synonym	19q13.11 microdeletion syndrome (en) monosomy 19q13.11 (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	A chromosomal deletion syndrome that has_material_basis_in a chromosome 19q13.11 deletion and that is characterized by characterized by poor overall growth, slender habitus, microcephaly, delayed development, intellectual disability with poor or absent speech, and feeding difficulties.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50938793

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